S7

S7 is a short synthetic peptide designed with balanced polar and hydrophobic residues to support structural adaptability. Its compact sequence allows exploration of binding motifs and conformational transitions in model systems. Researchers analyze its folding behavior through spectroscopic and computational approaches. Applications include motif screening, ligand-design development, and structure-activity studies.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.

CAT No: R2813

Synonyms/Alias:L-Leucine;L-leucyl-L-seryl-L-leucyl-L-isoleucyl-L-threonyl-L-arginyl;853248-13-2;S7 (trifluoroacetate salt);DTXSID40462527;(2S)-2-[[(2S)-2-[[(2S,3R)-2-[[(2S,3S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-amino-4-methylpentanoyl]amino]-3-hydroxypropanoyl]amino]-4-methylpentanoyl]amino]-3-methylpentanoyl]amino]-3-hydroxybutanoyl]amino]-5-(diaminomethylideneamino)pentanoyl]amino]-4-methylpentanoic acid

Custom Peptide Synthesis
cGMP Peptide
  • Registration of APIs
  • CMC information required for an IND
  • IND and NDA support
  • Drug master files (DMF) filing
M.F/Formula
C37H70N10O10
M.W/Mr.
815.01
Sequence
One Letter Code:LSLITRL
Three Letter Code:H-Leu-Ser-Leu-Ile-Thr-Arg-Leu-OH

S7, also known as Saccharide Compound 7, is a specialized carbohydrate blend designed for advanced research and development applications in the fields of biochemistry, molecular biology, and cellular studies. This compound features a unique arrangement of monosaccharide and oligosaccharide units, providing distinct physicochemical properties that make it highly versatile for laboratory investigations. Its structural complexity allows for precise manipulation in experimental protocols, enabling researchers to explore carbohydrate-mediated processes with enhanced specificity and reproducibility. S7 is characterized by its solubility, stability under various experimental conditions, and compatibility with a wide range of analytical techniques, making it an indispensable tool for scientists seeking to unlock the functional roles of carbohydrates in biological systems.

Glycobiology Research: S7 serves as a critical reagent in glycobiology, facilitating the study of carbohydrate-protein interactions, glycosylation pathways, and cell surface recognition events. Researchers utilize this compound to model glycan structures found in nature, enabling the dissection of complex biosynthetic routes and the identification of key enzymes involved in carbohydrate metabolism. Through its application, scientists can elucidate the mechanisms by which oligosaccharides modulate cellular communication, immune recognition, and pathogen-host interactions, providing foundational insights into the molecular language of cells.

Cell Culture and Differentiation Studies: In the context of cell culture, S7 is employed to modulate the extracellular environment, influencing cell adhesion, migration, and differentiation. By incorporating this carbohydrate compound into culture media or substrate coatings, investigators can mimic the glycan-rich microenvironments present in vivo, thereby promoting physiologically relevant cellular behaviors. Its use supports the investigation of stem cell fate decisions, tissue regeneration, and the development of organoid models, advancing our understanding of how specific carbohydrate cues guide cellular development and organization.

Drug Delivery and Nanotechnology: The unique structural features of S7 make it an attractive candidate for the design of drug delivery systems and nanomaterials. Its ability to form stable complexes with various biomolecules enables the creation of targeted delivery vehicles, where carbohydrate moieties facilitate selective binding to cellular receptors. Researchers exploit these properties to enhance the bioavailability and specificity of therapeutic agents, as well as to develop smart nanocarriers that respond to biological stimuli. S7 thus contributes to the advancement of precision medicine and the development of innovative therapeutic platforms.

Analytical Method Development: Analytical chemists leverage S7 as a standard or probe in the development and validation of carbohydrate detection methods. Its defined composition and reactivity make it suitable for optimizing chromatographic, spectroscopic, and mass spectrometric techniques used to analyze glycan structures in complex biological samples. By incorporating S7 into calibration protocols or as a reference compound, laboratories can achieve greater accuracy and reproducibility in glycomics research, supporting the identification and quantification of endogenous carbohydrates in diverse sample types.

Biomaterials Engineering: In the field of biomaterials, S7 is integrated into the design of hydrogels, scaffolds, and coatings to modulate material properties and biological interactions. Its incorporation enhances the biocompatibility and functionalization potential of synthetic matrices, enabling the creation of tissue engineering constructs that better mimic the natural extracellular matrix. Researchers utilize S7-modified materials to study cell-material interactions, promote tissue integration, and develop advanced wound healing solutions, highlighting its value in translational research and regenerative medicine.

S7's multifaceted applications underscore its importance as a research tool across diverse scientific disciplines. By enabling the study of glycobiology, supporting advanced cell culture models, powering innovations in drug delivery and nanotechnology, facilitating analytical method development, and advancing biomaterials engineering, it continues to drive progress at the interface of carbohydrate chemistry and biomedical science. As research into complex carbohydrate functions expands, S7 stands out as a reliable and versatile compound, empowering scientists to explore new frontiers in molecular biology and material science.

InChI
InChI=1S/C37H70N10O10/c1-10-21(8)28(46-32(52)25(15-19(4)5)43-33(53)27(17-48)45-30(50)23(38)14-18(2)3)34(54)47-29(22(9)49)35(55)42-24(12-11-13-41-37(39)40)31(51)44-26(36(56)57)16-20(6)7/h18-29,48-49H,10-17,38H2,1-9H3,(H,42,55)(H,43,53)(H,44,51)(H,45,50)(H,46,52)(H,47,54)(H,56,57)(H4,39,40,41)/t21-,22+,23-,24-,25-,26-,27-,28-,29-/m0/s1
InChI Key
LKGGSWKXVZZKJP-QQJGDSDLSA-N

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